Canonical Allele Identifier: PA2827678182
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1786652
ClinVar RCV Id: RCV002430617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Met716Val
CA399490578
NM_001352773.2:c.2146A>G